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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276574Erstellt: 24. Oktober 2026

Ethanolamine → 1-Aminocyclopentanemethanol

https://huagongshe.com/de/reaction/276574

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolamineHCID 700—
EduktAnilineHCID 6115—
EduktThionyl ChlorideHCID 24386—
Edukt4-Cyano-2-methylphenyl isothiocyanateHCID 18316299—
Produkt1-AminocyclopentanemethanolHCID 66307—
Produkt4-Amino-3-methylbenzonitrileHCID 7010316—
Produkt1-(Chloromethyl)cyclopentan-1-amine hydrochlorideHCID 69992485—

Reaktionsschritte

4-Cyano-2-methylaniline was synthesized as described in Method A1a. The aniline was converted to 4-cyano-2-methylphenyl isothiocyanate according to Method A2a, Step 3. 1-Amino-1-(hydroxymethyl)cyclopentane was synthesized as described in Method B1c. The 2-hydroxyethylamine was reacted with SOCl2 according to Method B7a to give 1-amino-1-(chloromethyl)cyclopentane HCl salt. The 2-chloroethylamine was reacted with 4-cyano-2-methylphenyl isothiocyanate according to Method C1a to give 2-(4-cyano-2-methylphenylimino)-1-thia-3-azaspiro[4.4]nonane. The thiazolidine was reacted with isobutyl bromide according to Method D2b to give 3-isobutyl-2-(4-iodo-2-methylphenylimino)-1-thia-3-azaspiro[4.4]nonane.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353006B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-e7c9bdddc8d9475398950b9579b3c4e2
Quellennotizuspto-grants-2002_03